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- Data Summary
SNP Report
Name | rs2293489 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr7:73107279(Fwd) | ||
Variant Alleles | C/T | ||
Ancestral Allele | C | ||
Functional Annotation | NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000430446; ENST00000432522; ENST00000436944; ENST00000421744; ENST00000428163; ENST00000430270) downstream_gene_variant(ENST00000478670; ENST00000441822) intron_variant(ENST00000432522; ENST00000496153; ENST00000430446; ENST00000423166; ENST00000436944; ENST00000421744; ENST00000442099; ENST00000453316; ENST00000428163; ENST00000423497; ENST00000265758; ENST00000430270; ENST00000487006) nc_transcript_variant(ENST00000496153; ENST00000463307; ENST00000487006) non_coding_exon_variant(ENST00000463307) upstream_gene_variant(ENST00000471215) |
||
No. of Studies | 0 (significant: 0; non-significant: 0; trend: 0) | ||
Source | LD-proxy |
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.